γδ T cell costimulatory ligands in antitumor immunity

Author:

McGraw Joseph M.1ORCID,Witherden Deborah A.2ORCID

Affiliation:

1. 1Department of Biology, Calibr at The Scripps Research Institute, La Jolla, CA 92037, USA

2. 2Department of Immunology and Microbiology, The Scripps Research Institute, La Jolla, CA 92037, USA

Abstract

Antitumor immunity relies on the ability of T cells to recognize and kill tumor targets. γδ T cells are a specialized subset of T cells that predominantly localizes to non-lymphoid tissue such as the skin, gut, and lung where they are actively involved in tumor immunosurveillance. γδ T cells respond to self-stress ligands that are increased on many tumor cells, and these interactions provide costimulatory signals that promote their activation and cytotoxicity. This review will cover costimulatory molecules that are known to be critical for the function of γδ T cells with a specific focus on mouse dendritic epidermal T cells (DETC). DETC are a prototypic tissue-resident γδ T cell population with known roles in antitumor immunity and are therefore useful for identifying mechanisms that may control activation of other γδ T cell subsets within non-lymphoid tissues. This review concludes with a brief discussion on how γδ T cell costimulatory molecules can be targeted for improved cancer immunotherapy.

Publisher

Open Exploration Publishing

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